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  • 1980-1984  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 2597-2603 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Photopolymerization of MMA was carried out at 40°C in bulk and in diluted systems using quinoline-chlorine (Q-Cl2) C.T. complex as the photoinitiator. Bulk polymerization followed normal free radical kinetics (initiator exponent = 0,5) for [Q-Cl2] 〈0,0015 mol.1-1. In diluted systems, variable monomer exponents were observed, ranging from slightly above 1 to 2,7, depending on the nature of the solvent (benzene, carbon tetrachloride, chloroform, chlorobenzene, acetone, dioxane, THF and DMF). Initiator exponent was ≤0,5 in diluted systems and it even became practically equal to zero depending on the nature of solvent and the level of dilution. The kinetic non-ideality in diluted systems was explained on the basis of solvent-retardation and initiator-termination via degradative chain transfer involving solvent-modified initiating complexes and chain radicals. The actual initiating complex appeared to be the (Q-Cl2)-monomer complex formed instantaneously in situ on addition of Q-Cl2 complex to the monomer.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Aqueous polymerization of MMA was kinetically studied using separately two complexes of sulfur dioxide as initiators, namely, quinoline-sulfur dioxide (Q-SO2) complex and tetrahydrofuran-sulfur dioxide (THF-SO2) complex. In each case the initiator exponent was 0,5 and the monomer exponent was 1,5. Kinetic data, inhibitory effect of hydroquinone, and incorporation of sulfoxy end groups in the polymers indicate a radical mechanism of polymerization with first order dependence on monomer for the rate of initiation while termination appears to take place bimolecularly.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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